D all participants provided written 
informed consent and all clinical investigations have been conducted according to the principles expressed in the according to the Helsinki declaration of human rights.Short-term primary colony assay in liquid culture mediumIn order to obtain in vitro EPC colonies, 36106 PBMC were seeded into Collagen I petri dishes (35 mm, Biocoat, BD Labware, Bedford, MA) by using three different culture media: i) M199 Glutamax I (Gibco BRL), supplemented with 20 of FCS, 1 penicillin/streptomycin and 1 L-glutamine; ii) long-term Medium 5100 (Voden, Milano, Italy), supplemented with 12.5 FBS, 12.5 HS, 1 L-glutamine, 1 penicillin-streptomycin; iii) EGM2 medium (Lonza, Walkersville, MD) with 2 FBS and full supplements (EGM2 Bullet kit, Lonza). Cultures were performed in triplicate and the detection of adherent colonies (id, aggregates with more than 50 cells) was monitored and scored as either 1326631 EPC/ ECFC or CFU-EC on the basis of morphological features, as previously described [6,25?7].Flow cytometric analysis of cultured EPC/ECFC and CFUECIn order to analyze the immunophenotypic pattern of primary EPC/ECFC and CFU-EC, cells were detached with trypsin/ EDTA (Gibco, BRL, UK) before the purchase Cucurbitacin I specific staining for flow cytometric analysis with the following Ab: CD45 Ab (2D1-APC), CD31 Ab (WM59-FITC), CD184 Ab (12G5-PE), CD105 Ab (SN6-PE), CD14 Ab (MWP9-PE), CD146 Ab (P1H12-PE) (all purchased from BD Biosciences Pharmingen), CD34 Ab (QBend/ 10-PercP; Serotec Ltd., Oxford) and CD133 Ab (AC133-PE; Miltenyi). Gate on viable cells was defined upon staining with 7amino-actinomycin D (7-AAD; BD Biosciences Pharmingen).Flow cytometric analysis of putative circulating EPCA four-color cytometry analysis of whole fresh peripheral blood (PB) samples was performed, as previously described [24], on a FACSCalibur equipped with the four-color option (Becton Dickinson, San Diego, CA), in order to enumerate the circulating EPC (CD34+/CD133+/VEGFR-2+/CD45- cells). Appropriate gate analysis was used for the detection of EPC excluding events of different origin, such as non-hematopoietic circulating cells and non-specifically stained events. At least 200.000 events were analyzed for each sample. The following antibodies (Ab) were used for FACS analysis: Flk-1/VEGF-R2 rabbit polyclonal IgG (Santa Cruz Biotechnology; Santa Cruz, CA) followed by anti-rabbit FITC Ab (DAKO, Milan, Italy); CD133 Ab (AC-133 PE; Miltenyi Biotech, Auburn, CA), CD45 Ab (2D1 APC or 2D1PercP; BD 
Biosciences Pharmingen,) and CD34 Ab (Q-Bend/10 PercP or QBend/10 APC; BD Biosciences Pharmingen).Fluorescence in situ hybridization (FISH)FISH analysis was carried out using an enumeration probe (i.e. Centromeric Probe CEP6 and CEP9) for a ploidy chromosome set evaluation. The probes were chosen from a commercially available list “Vysis FISH Chromosome probes” provided by Abbott Molecular (Abbott Park, IL). The FISH procedure was performed according to the manufacturer’s protocol. For each probe, 100 cells were evaluated. The cells were viewed through an epifluorescent microscope equipped with 100X oil objective lens and triple bandpass filter for DAPI, SpectrumGreen and Argipressin supplier SpectrumOrange.Immunocytochemical analysisImmunohistochemistry analysis was carried out by performing the alkaline phosphatase anti-alkaline-phosphatase (APAAP) staining, as previously described [26,27], using the following monoclonal Ab: Factor VIII Ab (F8/86; DAKO), CD31 (WM-59; BD), VEGF receptor-2 (KDR-1.D all participants provided written informed consent and all clinical investigations have been conducted according to the principles expressed in the according to the Helsinki declaration of human rights.Short-term primary colony assay in liquid culture mediumIn order to obtain in vitro EPC colonies, 36106 PBMC were seeded into Collagen I petri dishes (35 mm, Biocoat, BD Labware, Bedford, MA) by using three different culture media: i) M199 Glutamax I (Gibco BRL), supplemented with 20 of FCS, 1 penicillin/streptomycin and 1 L-glutamine; ii) long-term Medium 5100 (Voden, Milano, Italy), supplemented with 12.5 FBS, 12.5 HS, 1 L-glutamine, 1 penicillin-streptomycin; iii) EGM2 medium (Lonza, Walkersville, MD) with 2 FBS and full supplements (EGM2 Bullet kit, Lonza). Cultures were performed in triplicate and the detection of adherent colonies (id, aggregates with more than 50 cells) was monitored and scored as either 1326631 EPC/ ECFC or CFU-EC on the basis of morphological features, as previously described [6,25?7].Flow cytometric analysis of cultured EPC/ECFC and CFUECIn order to analyze the immunophenotypic pattern of primary EPC/ECFC and CFU-EC, cells were detached with trypsin/ EDTA (Gibco, BRL, UK) before the specific staining for flow cytometric analysis with the following Ab: CD45 Ab (2D1-APC), CD31 Ab (WM59-FITC), CD184 Ab (12G5-PE), CD105 Ab (SN6-PE), CD14 Ab (MWP9-PE), CD146 Ab (P1H12-PE) (all purchased from BD Biosciences Pharmingen), CD34 Ab (QBend/ 10-PercP; Serotec Ltd., Oxford) and CD133 Ab (AC133-PE; Miltenyi). Gate on viable cells was defined upon staining with 7amino-actinomycin D (7-AAD; BD Biosciences Pharmingen).Flow cytometric analysis of putative circulating EPCA four-color cytometry analysis of whole fresh peripheral blood (PB) samples was performed, as previously described [24], on a FACSCalibur equipped with the four-color option (Becton Dickinson, San Diego, CA), in order to enumerate the circulating EPC (CD34+/CD133+/VEGFR-2+/CD45- cells). Appropriate gate analysis was used for the detection of EPC excluding events of different origin, such as non-hematopoietic circulating cells and non-specifically stained events. At least 200.000 events were analyzed for each sample. The following antibodies (Ab) were used for FACS analysis: Flk-1/VEGF-R2 rabbit polyclonal IgG (Santa Cruz Biotechnology; Santa Cruz, CA) followed by anti-rabbit FITC Ab (DAKO, Milan, Italy); CD133 Ab (AC-133 PE; Miltenyi Biotech, Auburn, CA), CD45 Ab (2D1 APC or 2D1PercP; BD Biosciences Pharmingen,) and CD34 Ab (Q-Bend/10 PercP or QBend/10 APC; BD Biosciences Pharmingen).Fluorescence in situ hybridization (FISH)FISH analysis was carried out using an enumeration probe (i.e. Centromeric Probe CEP6 and CEP9) for a ploidy chromosome set evaluation. The probes were chosen from a commercially available list “Vysis FISH Chromosome probes” provided by Abbott Molecular (Abbott Park, IL). The FISH procedure was performed according to the manufacturer’s protocol. For each probe, 100 cells were evaluated. The cells were viewed through an epifluorescent microscope equipped with 100X oil objective lens and triple bandpass filter for DAPI, SpectrumGreen and SpectrumOrange.Immunocytochemical analysisImmunohistochemistry analysis was carried out by performing the alkaline phosphatase anti-alkaline-phosphatase (APAAP) staining, as previously described [26,27], using the following monoclonal Ab: Factor VIII Ab (F8/86; DAKO), CD31 (WM-59; BD), VEGF receptor-2 (KDR-1.
